Leukemia Research
Volume 26, Issue 11 , Pages 997-1005, November 2002

Increased circulating normal and BCR-ABL+Ve progenitor numbers in Philadelphia chromosome-positive acute myeloid leukaemia

  • Paul Baines

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK
    • Corresponding Author InformationCorresponding author. Tel.: +44-2920-743486; fax: +44-2920-744655.
  • ,
  • Steve Austin

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK
  • ,
  • Janet Fisher

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK
  • ,
  • Eleri Owen-Jones

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK
  • ,
  • Lisa Lee-Jones

      Affiliations

    • Institute of Medical Genetics, Cardiff, UK
  • ,
  • Duncan Throp

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK
  • ,
  • Mark Mckinley

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK
  • ,
  • Terry Hoy

      Affiliations

    • University of Wales College of Medicine, Cardiff, UK
  • ,
  • Ken Mills

      Affiliations

    • University of Wales College of Medicine, Cardiff, UK
  • ,
  • Peter W Thompson

      Affiliations

    • Institute of Medical Genetics, Cardiff, UK
  • ,
  • Alan K Burnett

      Affiliations

    • Haematology Department, University Hospital of Wales, Cardiff CF14 4XW, UK

Received 16 October 2001; accepted 9 February 2002.

Abstract 

We recorded elevated numbers of circulating myeloid and erythroid colony-forming cells in 15 adult patients with acute myeloid leukaemia (AML) who presented with high blood white cell counts. Since leukaemic blasts from three of these patients were Philadelphia chromosome-positive (Ph+), we were able to determine if blood progenitors from these particular patients arose from the leukaemic clone or from residual normal progenitors. Blasts and colonies were intensively investigated using a combination of cell surface marker analysis by flow cytometry, RT-PCR and interphase fluorescence in situ hybridization (FISH). FISH detected rearrangements within the major breakpoint BCR (M-BCR) region in blasts and in some myeloid and erythroid colonies from patients 1 and 2. The minor breakpoint (m-BCR) region was detected in blasts and in some myeloid and erythroid colonies from patient 3. RT-PCR detected long b2a2 BCR-ABL transcripts in blasts from patients 1 and 2, although misspliced short e1a2 transcripts were also seen in patient 1. Only e1a2 transcripts were found in blasts from patient 3. Flow sorting demonstrated the B-cell marker CD19 on blasts and on a proportion of myeloid and erythroid progenitors from patients 1 and 3. RT-PCR also detected IgH rearrangements, further evidence of B-cell differentiation, in blasts from these two patients. We conclude that both normal and clonal circulating progenitor numbers can be raised in both M-BCR and m-BCR Ph+ AML. The underlying cause, perhaps efflux from a congested marrow, may be common to AML patients with a high blood white cell count.

Abbreviations:  AML, acute myeloid leukaemia, CML, chronic myeloid leukaemia, GMCFC, granulocyte–monocyte colony-forming cells, FISH, interphase fluorescence in situ hybridization, MNC, mononuclear cells, Ph+, Philadelphia chromosome-positive, RT-PCR, reverse transcriptase polymerase chain reaction

Keywords:  BCR-ABL, AML, Colony-forming progenitors, FISH, RT-PCR

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PII: S0145-2126(02)00049-8

Leukemia Research
Volume 26, Issue 11 , Pages 997-1005, November 2002